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Literature summary for 3.4.21.1 extracted from

  • Abell, A.D.; Nabbs, B.K.
    Ring-deactivated hydroxymethylpyrroles as inhibitors of alpha-chymotrypsin (2001), Bioorg. Med. Chem., 9, 621-628.
    View publication on PubMed

Inhibitors

Inhibitors Comment Organism Structure
2-hydroxymethyl-1-(2-phenylethanecarbonyl)pyrrole 0.0125 mg/ml, 10% inhibition Bos taurus
2-hydroxymethyl-1-(2-phenylethansulfonyl)pyrrole 0.0125 mg/ml, 15% inhibition Bos taurus
2-hydroxymethyl-1-(2-phenylethenylsulfonyl)pyrrole 0.0125 mg/ml, 15% inhibition Bos taurus
2-hydroxymethyl-1-(N-phthalyl-L-leucine)pyrrole 0.0125 mg/ml, 10% inhibition Bos taurus
2-hydroxymethyl-1-(phenylsulfonyl)pyrrole 0.053 mM, 20% inhibition Bos taurus
methyl-4-hydroxy-4-[1-(phenylsulfonyl)pyrrol-2-yl]butanoate 0.0125 mg/ml, 10% inhibition Bos taurus

Organism

Organism UniProt Comment Textmining
Bos taurus
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-
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Substrates and Products (Substrate)

Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
N-succinyl-L-Phe-p-nitroanilide + H2O
-
Bos taurus N-succinyl-L-Phe + p-nitroaniline
-
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